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Clinical Trials/NCT00000249
NCT00000249CompletedPhase 2

Effects of Subanesthetic Concentrations of Nitrous Oxide

University of Chicago1 site in 1 country10 target enrollmentStarted: September 1993Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
Pain intensity

Study Overview

Brief Summary

The purpose of this study is to conduct experiments to examine subjective and reinforcing effects of nitrous oxide. Mood altering and psychomotor effects will be tested on non-drug abusers and preference procedures will be used to assess reinforcing effects. To examine effects of subanesthetic concentrations of nitrous oxide on cold-pressor pain in humans.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
21 Years to 37 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

20% N2O

Active Comparator

Subject inhaled 20% N2O for 40 minutes with cold immersion at 10 & 30 minutes

Intervention: 20% N2O (Drug)

30% N2O

Active Comparator

Subject inhaled 30% N2O for 40 minutes with cold immersion at 10 and 30 minutes

Intervention: 30% N2O (Drug)

40% N2O

Active Comparator

Subject inhaled 40% N2O for 40 minutes with cold immersion at 10 and 30 minutes

Intervention: 40% N2O (Drug)

Outcomes

Primary Outcomes

Pain intensity

Time Frame: during cold test at 10 min & 30 min of inhalation

Subjects immersed non-dominant arm for 3 minutes twice in 2-3 degree C water while inhaling 0 (placebo), 20, 30, or 40% N2O for a total of 40 minutes

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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